Taiwan FDA registration aea6b638eb32af09bb681752146fcf07
"Covidien" Yarrow Extension Fittings Set (Sterilized)
TW: “柯惠” 亞羅延伸管件組 (滅菌)
Taiwan·Risk Class 1·COVIDIEN LLC;; COVIDIEN IRELAND LIMITED·Registered Jun 29, 2010 – Jun 29, 2015CancelledRegistration details
- Analysis ID
- aea6b638eb32af09bb681752146fcf07
- Customs Code
- DHA04400895200
Company information
- Manufacturer
- COVIDIEN LLC;; COVIDIEN IRELAND LIMITED
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4200 Incoming/Drainage Tubes and Accessories
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 29, 2010
- Expiry Date
- Jun 29, 2015
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" Yarrow Extension Fittings Set (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aea6b638eb32af09bb681752146fcf07 and manufactured by COVIDIEN LLC;; COVIDIEN IRELAND LIMITED. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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